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1083-59-6

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1083-59-6 Usage

Structure

A pyrimidine derivative containing a furan ring with a nitro group attached

Usage

As a building block in the synthesis of various pharmaceuticals and chemical compounds

Potential applications

Antimicrobial and antifungal agent

Bioactivity

The presence of the nitro group makes it a potential candidate for reduction to form a nitroso compound, which can have biological significance as a bioactive molecule

Versatility

A versatile compound with potential applications in pharmaceutical and chemical industries

Check Digit Verification of cas no

The CAS Registry Mumber 1083-59-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,8 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1083-59:
(6*1)+(5*0)+(4*8)+(3*3)+(2*5)+(1*9)=66
66 % 10 = 6
So 1083-59-6 is a valid CAS Registry Number.

1083-59-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(5-nitrofuran-2-yl)ethenyl]pyrimidine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1083-59-6 SDS

1083-59-6Downstream Products

1083-59-6Relevant articles and documents

Chemotherapeutic nitroheterocycles. Antischistosomal properties of nitrofurylvinyl and nitrothienylvinyl heterocycles

Henry,Brown,Cory,et al.

, p. 1287 - 1291 (2007/10/05)

A series of 24 analogs of the experimental antischistosomal agent, 5 amino 3 [2 (5 nitro 2 furyl) vinyl] 1,2,4 oxadiazole, was prepared and evaluated in mice infected with Schistosoma mansoni. Although antischistosomal activity was widespread in the series, only four of the compounds showed significant curative properties. Compounds containing 2 imidazolyl and 2 pyridyl groups gave cure rates around 25% at 400 and 250 mg/kg dose levels, respectively. The 2 thiazolyl and 2 pyrimidyl derivatives were especially notable, yielding 100% cures at 250 and 200 mg/kg dose levels, respectively.

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